Cingulin, paracingulin, and PLEKHA7: signaling and cytoskeletal adaptors at the apical junctional complex

被引:50
作者
Citi, Sandra [1 ]
Pulimeno, Pamela [1 ]
Paschoud, Serge [1 ]
机构
[1] Univ Geneva, Dept Mol Biol, CH-1211 Geneva 4, Switzerland
来源
BARRIERS AND CHANNELS FORMED BY TIGHT JUNCTION PROTEINS I | 2012年 / 1257卷
关键词
cingulin; paracingulin; PLEKHA7; ZO-1; p120ctn; junctions; TIGHT JUNCTIONS; PROTEIN CINGULIN; EPITHELIAL-CELLS; BLOOD-PRESSURE; PERIPHERAL COMPONENT; STRATIFIED EPITHELIA; ADHERENS JUNCTIONS; GENE-EXPRESSION; ZO-1; INTERACTS;
D O I
10.1111/j.1749-6632.2012.06506.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Cingulin, paracingulin, and PLEKHA7 are proteins localized in the cytoplasmic region of the apical junctional complex of vertebrate epithelial cells. Cingulin has been detected at tight junctions (TJs), whereas paracingulin has been detected at both TJs and adherens junctions (AJs) and PLEKHA7 has been detected at AJs. One function of cingulin and paracingulin is to regulate the activity of Rho family GTPases at junctions through their direct interaction with guanidine exchange factors of RhoA and Rac1. Cingulin also contributes to the regulation of transcription of several genes in different types of cultured cells, in part through its ability to modulate RhoA activity. PLEKHA7, together with paracingulin, is part of a protein complex that links E-cadherin to the microtubule cytoskeleton at AJs. In this paper, we review the current knowledge about these proteins, including their discovery, the characterization of their expression, localization, structure, molecular interactions, and their roles in different developmental and disease model systems.
引用
收藏
页码:125 / 132
页数:8
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